M. Anne Spence

12.0k total citations
157 papers, 6.3k citations indexed

About

M. Anne Spence is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, M. Anne Spence has authored 157 papers receiving a total of 6.3k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Genetics, 51 papers in Molecular Biology and 35 papers in Cognitive Neuroscience. Recurrent topics in M. Anne Spence's work include Autism Spectrum Disorder Research (31 papers), Genetics and Neurodevelopmental Disorders (23 papers) and Genomic variations and chromosomal abnormalities (17 papers). M. Anne Spence is often cited by papers focused on Autism Spectrum Disorder Research (31 papers), Genetics and Neurodevelopmental Disorders (23 papers) and Genomic variations and chromosomal abnormalities (17 papers). M. Anne Spence collaborates with scholars based in United States, Canada and United Kingdom. M. Anne Spence's co-authors include Pamela Flodman, Joan R. Westlake, Kenneth K. Kídd, Robert K. Moyzis, James M. Swanson, Deborah Grady, R S Sparkes, Pauline A. Filipek, Moyra Smith and Nancy J. Minshew and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and JAMA.

In The Last Decade

M. Anne Spence

156 papers receiving 5.9k citations

Peers

M. Anne Spence
Michael L. Cuccaro United States
Sven Cichon Germany
Pamela Sklar United States
Matthew W. State United States
Isabelle Rapin United States
Michael J. Owen United Kingdom
Kieran C. Murphy United Kingdom
Michael L. Cuccaro United States
M. Anne Spence
Citations per year, relative to M. Anne Spence M. Anne Spence (= 1×) peers Michael L. Cuccaro

Countries citing papers authored by M. Anne Spence

Since Specialization
Citations

This map shows the geographic impact of M. Anne Spence's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by M. Anne Spence with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Anne Spence more than expected).

Fields of papers citing papers by M. Anne Spence

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Anne Spence. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by M. Anne Spence. The network helps show where M. Anne Spence may publish in the future.

Co-authorship network of co-authors of M. Anne Spence

This figure shows the co-authorship network connecting the top 25 collaborators of M. Anne Spence. A scholar is included among the top collaborators of M. Anne Spence based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. Anne Spence. M. Anne Spence is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Spence, M. Anne, et al.. (2023). Rhythmic chew cycles with distinct fast and slow phases are ancestral to gnathostomes. Philosophical Transactions of the Royal Society B Biological Sciences. 378(1891). 20220539–20220539. 5 indexed citations
2.
Fujikawa-Brooks, Sharon, A. Lisette Isenberg, Kathryn Osann, M. Anne Spence, & Nicole M. Gage. (2010). The effect of rate stress on the auditory brainstem response in autism: A preliminary report. International Journal of Audiology. 49(2). 129–140. 25 indexed citations
3.
Flodman, Pamela, et al.. (2008). Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA). American Journal of Medical Genetics Part A. 146A(7). 833–842. 40 indexed citations
4.
Harris, Adrian L. & M. Anne Spence. (2007). 'Disturbing the Complacency of Religion'? The Evangelical Crusades of Dr Billy Graham and Father Patrick Peyton in Britain, 1951-54. Twentieth Century British History. 18(4). 481–513. 8 indexed citations
5.
Goldberg, Wendy A., et al.. (2007). Use of Home Videotapes to Confirm Parental Reports of Regression in Autism. Journal of Autism and Developmental Disorders. 38(6). 1136–1146. 42 indexed citations
6.
Schellenberg, Gerard D., Géraldine Dawson, Yun Ju Sung, et al.. (2006). Evidence for multiple loci from a genome scan of autism kindreds. Molecular Psychiatry. 11(11). 1049–1060. 94 indexed citations
7.
Filipek, Pauline A., Moyra Smith, Maureen Bocian, et al.. (2003). Mitochondrial dysfunction in autistic patients with 15q inverted duplication. Annals of Neurology. 53(6). 801–804. 109 indexed citations
8.
Grady, Deborah, M. Smith, Eunice S. Wang, et al.. (2003). High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder. Molecular Psychiatry. 8(5). 536–545. 104 indexed citations
9.
Ding, Yuan-Chun, Deborah Grady, Atsuyuki Morishima, et al.. (2001). Evidence of positive selection acting at the human dopamine receptor D4 gene locus. Proceedings of the National Academy of Sciences. 99(1). 309–314. 377 indexed citations
10.
Bristol, Marie M., Donald J. Cohen, E. Jane Costello, et al.. (1996). State of the science in autism: Report to the National institutes of health. Journal of Autism and Developmental Disorders. 26(2). 121–154. 108 indexed citations
11.
Bateman, J. Bronwyn, Rita M. Cantor, Camilla Heinzmann, et al.. (1993). 2×0.30ST钢丝帘线的开发. PubMed Central. 30(7). 299–434. 3 indexed citations
12.
O’Hanlon, Karen, Karen Weissbecker, Victoria K. Cortessis, M. Anne Spence, & Edwin A. Azen. (1988). Genes for salivary proline-rich proteins and taste for phenylthiourea are not closely linked in humans. Cytogenetic and Genome Research. 49(4). 315–317. 4 indexed citations
13.
Crist, Michol, et al.. (1985). Glutamate Pyruvate Transaminase Null Allele (GPT°) in the Navajo. Human Heredity. 35(1). 59–61. 2 indexed citations
14.
Sparkes, R S, M. Anne Spence, Robert G. Gray, et al.. (1985). Genetic Linkage Analysis of the Carpal Tunnel Syndrome. Human Heredity. 35(5). 288–291. 9 indexed citations
15.
Sparkes, R S, L. Leigh Field, M.C. Sparkes, et al.. (1984). Genetic Linkage Studies of Transf errin, Pseudocholinesterase, and Chromosome 1 Loci. Human Heredity. 34(2). 96–100. 23 indexed citations
16.
Field, L. Leigh, J. R. Heckenlively, R.S. Sparkes, et al.. (1982). Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosa.. Journal of Medical Genetics. 19(4). 266–270. 25 indexed citations
17.
Field, L. Leigh, J. R. Heckenlively, R.S. Sparkes, et al.. (1980). Linkage analysis of several families with dominant form retinitis pigmentosa. The American Journal of Human Genetics. 32(6). 105. 1 indexed citations
18.
Spence, M. Anne & Frederick W. Luthardt. (1975). Mitotic association patterns of nucleolar organizing chromosomes in the mouse. Cytogenetic and Genome Research. 15(4). 276–280. 5 indexed citations
19.
Spence, M. Anne, et al.. (1974). Dermatoglyphics of Childhood Psychosis: A Family Study. Human Heredity. 24(1). 82–87. 6 indexed citations
20.
Spence, M. Anne, Robert C. Elston, K.K. Namboodiri, & William S. Pollitzer. (1973). Evidence for a Possible Major Gene Effect in Absolute Finger Ridge Count. Human Heredity. 23(5). 414–421. 32 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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